JP6026139B2 - Composition for photo-alignment film and optical anisotropic film - Google Patents

Description

  The present invention relates to a novel composition for a photo-alignment film and a composition for an optically anisotropic film, and further relates to various optically anisotropic films, optical materials, and liquid crystal cells obtained by using the composition.

  In recent years, in the field of displays (including flexible displays as well as liquid crystal displays), various optical anisotropic films such as retardation films, viewing angle enhancement films, brightness enhancement films, polarizing films, conductive materials, nonlinear optical materials, Various optical materials such as photoreactive actuators are used in various forms. Such an optically anisotropic film or optical material is produced by orienting a liquid crystalline compound, a dye, a conductive compound or the like on a layer having orientation ability (film, substrate surface, etc.). As a method of providing a layer, a method of chemically or physically treating a surface is known. As such a method, for example, a rubbing process in which a polymer resin film such as polyimide coated on a substrate surface is rubbed in one direction with a cloth is known and used for forming an alignment film for a liquid crystal display device or the like. .

  However, in such a method, contamination of the liquid crystal production line due to the generation of fine dust, destruction of TFT (thin film transistor) elements due to static electricity, etc. may cause a decrease in yield in the manufacturing process of the liquid crystal panel. There is a problem that it is difficult to control the general orientation.

  Therefore, instead of rubbing treatment, various studies have been made on the production of photo-alignment films having alignment ability such as liquid crystals using photoreactive compounds (compounds that undergo photoisomerization, photodimerization, photolysis, etc. by light irradiation). Has been. For example, as a compound causing photoisomerization, an azobenzene compound having an azo group (Non-patent Document 1), and as a compound causing photodimerization, a cinnamic acid derivative having a cinnamoyl group (Non-patent Document 2), a coumarin having a coumarin group. Photodegradable polyimide (Non-Patent Document 5) and the like are known as compounds that cause photolysis, such as a derivative (Non-Patent Document 3) and a chalcone derivative having a chalcone group (Non-Patent Document 4).

  However, since the skeletons that exhibit photoisomerization, dimerization, or photolysis are limited in this way, there has been a problem that the degree of freedom in material selection is low in the production of photoalignment films.

  The Fries rearrangement is a rearrangement reaction that produces ortho- and / or para-phenol ketone from a phenol ester, and is catalyzed by a Lewis acid (Non-patent Document 6). Of the fleece dislocations, those that proceed by light are called optical fleece dislocations. The reaction mechanism of the photo-Fries rearrangement is considered to be as follows via a radical.

K. Ichimura et al., Langmuir, vol.4, page 1214 (1988) M. Schadt et al., J. Appl. Phys., Vol.31, No.7, page 2155 (1992) M. Schadt et al., Nature., Vol. 381, page 212 (1996) Toshihiro Ogawa et al., Proceedings of Liquid Crystal Panel Discussion, 2AB03 (1997) Proc. Of the 22nd Liquid Crystal Symposium, 1672 A17 (1996) THE MERCK INDEX FOURTEENTH EDITION, Organic Name Reactions 150

  In the above background, the present invention provides a composition for a photo-alignment film containing a photoreactive compound having a very high degree of freedom in material selection. The present invention also provides a photo-alignment film using the composition for photo-alignment film. Furthermore, the present invention provides a retardation film, a viewing angle enhancement film, a brightness enhancement film, a polarizing film, and other optical anisotropic films and conductive materials, nonlinear optical materials, photoreactive actuators, and the like using the photo-alignment film. And various liquid crystal cells using the photo-alignment film.

  In addition, the present invention provides a composition for an optically anisotropic film containing the photoreactive compound, and an optically anisotropic film using the composition.

  As a result of diligent research, the present inventors have determined that a photoreactive polymer having a photoreactive group having a thiophenolic ester group, which is represented by the following formula, at the end of the side chain of the polymer as a photoreactive compound. We have found that the above-mentioned problems can be solved by using and have further studied and completed the present invention.

（式中，環Ａは非置換若しくは置換脂環式炭化水素又は非置換若しくは置換芳香環であり，環Ｂは非置換若しくは置換芳香環である。）

(Wherein ring A is an unsubstituted or substituted alicyclic hydrocarbon or unsubstituted or substituted aromatic ring, and ring B is an unsubstituted or substituted aromatic ring.)

  In the photoreactive polymer of the present invention, the thiophenolic ester group in the side chain is irradiated with light and becomes a decomposition product via a radical by photocleavage. Furthermore, when the ortho position (or para position) of the thiol group of ring B is unsubstituted, a part of these radicals undergo photofleece rearrangement to produce ortho-thiophenol ketone (or para-thiophenol ketone). To do. Therefore, when a composition for a photo-alignment film or an optically anisotropic film containing the photoreactive polymer is applied to a base material and light is irradiated to this, light that causes these series of reactions is prepared. When linearly polarized light is used, only the thiophenolic ester group that exists coaxially with the polarization axis of the linearly polarized light causes selective photocleavage or photocleavage and photofleece rearrangement. Thereby, the photo-alignment film or optically anisotropic film provided with alignment ability, such as a liquid crystal, can be manufactured. The present invention has been completed based on such findings.

〔式中，Ｍはホモポリマー又はコポリマーの主鎖を形成するモノマー単位であり，ＳＰＣＲはスペーサー単位であり，環Ａは非置換若しくは置換脂環式炭化水素又は非置換若しくは置換芳香環であり，環Ｂは非置換若しくは置換芳香環であり，Ｚはアルキル基，アルコキシ基，シアノ基，ニトロ基，ハロゲン原子，−ＣＨ＝ＣＨＺ¹，−Ｃ≡ＣＺ¹（但し，Ｚ¹はアルキル基，アルコキシ基，アルコキシカルボニル基，アルコキシスルホニル基，シアノ基，ニトロ基又はハロゲン原子である。），−ＣＯＯＺ²，又は−ＳＯ₃Ｚ²（但し，Ｚ²はアルキル基である。）であり、ｎは０又は１である。〕
で示される繰り返し単位を有する光反応性ポリマーを含んでなる，光配向膜用組成物，
〔２〕環Ａの置換基及び環Ｂの置換基が，それぞれ独立に，アルキル基，アルコキシ基，シアノ基，ニトロ基及びハロゲン原子からなる群から選ばれる１又は２以上の基である，上記〔１〕の光配向膜用組成物，
〔３〕Ｍが，アクリレート，メタクリレート，２−クロロアクリレート，２−フェニルアクリレート，アクリロイルフェニレン，アクリルアミド，メタクリアミド，２−クロロアクリルアミド，２−フェニルアクリルアミド，ビニルエーテル，スチレン誘導体，ビニルエステル，マレイン酸誘導体，フマル酸誘導体，シロキサン，エポキシドからなる群から選ばれる１又は２種以上のモノマー単位であり，
ＳＰＣＲが，−（ＣＨ₂）p−（但し，ｐは１〜１２のいずれかの整数である。），１，２−プロピレン，１，３−ブチレン，シクロペンタン−１，２−ジイル，シクロペンタン−１，３−ジイル，シクロヘキサン−１，３−ジイル，シクロヘキサン−１，４−ジイル，ピペリジン−１，４−ジイル，ピペラジン−１，４−ジイル，１，２−フェニレン，１，３−フェニレン，１，４−フェニレンからなる群から選ばれるスペーサー単位であり，
環Ａが，

〔但し，Ｘ^1A〜Ｘ^42Aは，それぞれ独立して，水素原子，アルキル基，アルコキシ基，ハロゲン原子又はシアノ基である。〕
で示されるいずれかの基であり，
環Ｂが，

〔但し，Ｘ^1B〜Ｘ^40Bは，それぞれ独立して，水素原子，アルキル基，アルコキシ基，ハロゲン原子又はシアノ基であり，Ｘは，窒素原子，酸素原子，硫黄原子である。〕
で示されるいずれかの基である，上記〔１〕の光配向膜用組成物，
〔４〕Ｘ^1BとＸ^4Bの少なくとも一方，Ｘ^5BとＸ^12Bの少なくとも一方，Ｘ^13BとＸ^24Bの少なくとも一方，Ｘ^25BとＸ^30Bの少なくとも一方，Ｘ^31BとＸ^38Bの少なくとも一方，及び，Ｘ^39Bが水素原子である，上記〔３〕の光配向膜用組成物，
〔５〕一般式（Ｉ−ａ）

〔式中，Ｒは，水素原子，メチル基，フェニル基又は塩素原子であり，Ｘ^1A〜Ｘ^4A及びＸ^1B〜Ｘ^4Bの各々は，それぞれ独立して，水素原子，アルキル基，アルコキシ基，ハロゲン原子又はシアノ基であり，Ｚは，アルキル基，アルコキシ基，シアノ基，ニトロ基，ハロゲン原子，−ＣＨ＝ＣＨＺ¹，−Ｃ≡ＣＺ¹（但し，Ｚ¹はアルキル基，アルコキシ基，アルコキシカルボニル基，アルコキシスルホニル基，シアノ基，ニトロ基又はハロゲン原子である。），−ＣＯＯＺ²，又は−ＳＯ₃Ｚ²（但し，Ｚ²はアルキル基である。）であり，ｐは，１〜１２のいずれかの整数であり、ｎは０又は１である。〕
で示される繰り返し単位を有する光反応性ポリマーを含んでなる，光配向膜用組成物，
〔６〕Ｘ^1BとＸ^4Bの少なくとも一方が水素原子である，上記〔５〕の光配向膜用組成物，
〔７〕上記〔１〕〜〔６〕のいずれかの光配向膜用組成物を基材表面に塗布したものを準備し，これに直線偏光を照射してなる，光配向膜，
〔８〕上記〔７〕の光配向膜に，液晶性化合物，色素又は導電性化合物を配向させてなる，光学異方性フィルム又は光学材料，
〔９〕上記〔７〕の光配向膜２枚を，一方の光配向膜における直線偏光照射時の偏光軸の方向と，他方の光配向膜における直線偏光照射時の偏光軸の方向が，互いに所定の角度をなすように対向させ，該対向させた光配向膜の間に液晶性化合物を充填してなる，液晶セル，
〔１０〕一般式（Ｉ）

〔式中，Ｍはホモポリマー又はコポリマーの主鎖を形成するモノマー単位であり，ＳＰＣＲはスペーサー単位であり，環Ａは非置換若しくは置換脂環式炭化水素又は非置換若しくは置換芳香環であり，環Ｂは非置換若しくは置換芳香環であり，Ｚはアルキル基，アルコキシ基，シアノ基，ニトロ基，ハロゲン原子，−ＣＨ＝ＣＨＺ¹，−Ｃ≡ＣＺ¹（但し，Ｚ¹はアルキル基，アルコキシ基，アルコキシカルボニル基，アルコキシスルホニル基，シアノ基，ニトロ基又はハロゲン原子である。），−ＣＯＯＺ²，又は−ＳＯ₃Ｚ²（但し，Ｚ²はアルキル基である。）であり、ｎは０又は１である。〕
で示される繰り返し単位を有する光反応性ポリマーを含んでなる，光学異方性フィルム用組成物，
〔１１〕上記〔１０〕の光学異方性フィルム用組成物を基材表面に塗布したものを準備し，これに直線偏光を照射した後，該光学異方性フィルム用組成物に含まれる液晶性化合物が液晶状態を示す温度以上に加熱し，更に該液晶性化合物が液晶状態を示す温度未満に冷却してなる，光学異方性フィルム，
に関する。 That is, the present invention
[1] General formula (I)

[Wherein M is a monomer unit forming the main chain of the homopolymer or copolymer, SPCR is a spacer unit, ring A is an unsubstituted or substituted alicyclic hydrocarbon or an unsubstituted or substituted aromatic ring, ring B is an unsubstituted or substituted aromatic ring, Z is an alkyl group, an alkoxy group, a cyano group, a nitro group, a halogen ^{atom, -CH = CHZ 1, -C≡CZ 1} ( where, Z ¹ is an alkyl group, an alkoxy A group, an alkoxycarbonyl group, an alkoxysulfonyl group, a cyano group, a nitro group, or a halogen atom), —COOZ ² , or —SO ₃ Z ² (wherein Z ² is an alkyl group), and n is 0 or 1. ]
A composition for a photoalignment film, comprising a photoreactive polymer having a repeating unit represented by:
[2] The ring A substituent and the ring B substituent are each independently one or more groups selected from the group consisting of an alkyl group, an alkoxy group, a cyano group, a nitro group, and a halogen atom, [1] Composition for photo-alignment film,
[3] M is acrylate, methacrylate, 2-chloroacrylate, 2-phenylacrylate, acryloylphenylene, acrylamide, methacrylamide, 2-chloroacrylamide, 2-phenylacrylamide, vinyl ether, styrene derivative, vinyl ester, maleic acid derivative, One or more monomer units selected from the group consisting of fumaric acid derivatives, siloxanes, and epoxides,
SPCR is — (CH ₂ ) p — (where p is an integer of 1 to 12), 1,2-propylene, 1,3-butylene, cyclopentane-1,2-diyl, cyclo Pentane-1,3-diyl, cyclohexane-1,3-diyl, cyclohexane-1,4-diyl, piperidine-1,4-diyl, piperazine-1,4-diyl, 1,2-phenylene, 1,3- A spacer unit selected from the group consisting of phenylene and 1,4-phenylene,
Ring A is

[However, X ^{1A to} X ^42A each independently represents a hydrogen atom, an alkyl group, an alkoxy group, a halogen atom, or a cyano group. ]
Any of the groups represented by
Ring B is

[However, X ^{1B to} X ^40B are each independently a hydrogen atom, an alkyl group, an alkoxy group, a halogen atom, or a cyano group, and X is a nitrogen atom, an oxygen atom, or a sulfur atom. ]
A composition for a photoalignment film according to the above [1], which is any group represented by
[4] At least one of X ^1B and X ^4B , at least one of X ^5B and X ^12B , at least one of X ^13B and X ^24B , at least one of X ^25B and X ^30B , at least one of X ^31B and X ^38B , and ^X39B is a hydrogen atom, The composition for photo-alignment films of said [3],
[5] General formula (Ia)

[Wherein, R represents a hydrogen atom, a methyl group, a phenyl group or a chlorine atom, and each of X ^{1A to} X ^4A and X ^{1B to} X ^4B independently represents a hydrogen atom, an alkyl group, an alkoxy group, a halogen atom or a cyano group, Z is an alkyl group, an alkoxy group, a cyano group, a nitro group, a halogen ^{atom, -CH = CHZ 1, -C≡CZ 1} ( where, Z ¹ is an alkyl group, an alkoxy group, an alkoxy A carbonyl group, an alkoxysulfonyl group, a cyano group, a nitro group, or a halogen atom.), —COOZ ² , or —SO ₃ Z ² (wherein Z ² is an alkyl group), and p is 1 to 1 Any integer of 12 and n is 0 or 1. ]
A composition for a photoalignment film, comprising a photoreactive polymer having a repeating unit represented by:
[6] The composition for photoalignment film according to [5], wherein at least one of X ^1B and X ^4B is a hydrogen atom,
[7] A photo-alignment film prepared by applying a composition for a photo-alignment film according to any one of [1] to [6] above to a substrate surface, and irradiating it with linearly polarized light,
[8] An optically anisotropic film or optical material obtained by aligning a liquid crystalline compound, a dye or a conductive compound on the photoalignment film of [7] above,
[9] The two photo-alignment films of [7] described above are such that the direction of the polarization axis when linearly polarized light is irradiated on one photoalignment film and the direction of the polarization axis when linearly polarized light is irradiated on the other photo-alignment film are mutually A liquid crystal cell having a predetermined angle facing each other and a liquid crystal compound filled between the facing photo-alignment films;
[10] General formula (I)

[Wherein M is a monomer unit forming the main chain of the homopolymer or copolymer, SPCR is a spacer unit, ring A is an unsubstituted or substituted alicyclic hydrocarbon or an unsubstituted or substituted aromatic ring, ring B is an unsubstituted or substituted aromatic ring, Z is an alkyl group, an alkoxy group, a cyano group, a nitro group, a halogen ^{atom, -CH = CHZ 1, -C≡CZ 1} ( where, Z ¹ is an alkyl group, an alkoxy A group, an alkoxycarbonyl group, an alkoxysulfonyl group, a cyano group, a nitro group, or a halogen atom), —COOZ ² , or —SO ₃ Z ² (wherein Z ² is an alkyl group), and n is 0 or 1. ]
An optically anisotropic film composition comprising a photoreactive polymer having a repeating unit represented by:
[11] The liquid crystal contained in the composition for optically anisotropic film is prepared by applying the optically anisotropic film composition of [10] above to the surface of the base material, and irradiating it with linearly polarized light. An optically anisotropic film obtained by heating above the temperature at which the crystalline compound exhibits a liquid crystal state and further cooling to a temperature below which the liquid crystalline compound exhibits a liquid crystal state;
About.

  The present invention provides a composition for a photo-alignment film and a composition for an optically anisotropic film using a new generation mechanism of photo-cleavage and photo-fleece dislocation, and a conventional photo-alignment group (for example, The thiophenolic ester group, which has a simpler structure regardless of azo group, cinnamoyl group, chalcone group, coumarin group, etc.), is used as a photo-alignment group. The degree of freedom is greatly improved.

  In addition, the composition for optically anisotropic film of the present invention does not require a separate alignment film, and thus has an advantage that an optically anisotropic film can be obtained simply and at low cost.

  Furthermore, the composition for photo-alignment films and the composition for optically anisotropic films of the present invention have an excellent feature that coloring due to exposure (irradiation with linearly polarized light) can be suppressed.

The thin film made of a photo-alignment film composition 1 of Example 1, with the state irradiated with linearly polarized light and an irradiation dose of 60 J / cm ² unirradiated state (0J / cm ^2), the change of the thin film These are the results of observation by microinfrared spectroscopy.

〔式中，記号は前記と同一意味を有する。〕
で示される繰り返し単位を有する光反応性ポリマー。 In the photoreactive polymer (I) according to the present invention, preferred specific examples are shown below.
Formula (Ia)

[Wherein the symbols have the same meaning as described above. ]
A photoreactive polymer having a repeating unit represented by:

  In general formula (I) (including general formula (Ia) if the same applies to general formula (Ia), the same shall apply hereinafter), M is a monomer that forms the main chain of a homopolymer or copolymer. Any monomer unit generally used in this field can be suitably used. Examples of such monomer units include acrylate, methacrylate, 2-chloroacrylate, 2-phenylacrylate, acrylamide, methacrylamide, 2-chloroacrylamide, 2-phenylacrylamide, vinyl ether, styrene derivatives (for example, α-methylstyrene). , P-styrene sulfonate), maleic acid derivatives (for example, maleic acid ester, phenyl maleimide, cyclohexyl maleimide), fumaric acid derivatives (for example, fumaric acid ester), siloxane, and epoxide. A monomer unit is mentioned. When M consists of one monomer unit, the photoreactive polymer of general formula (I) is a homopolymer, and when M consists of two or more monomer units, the photoreactive polymer of general formula (I) is A copolymer. When the photoreactive polymer according to the present invention is a copolymer, the copolymer includes any of alternating type, random type, and graft type. Of these monomer units, acrylate and methacrylate are preferred.

SPCR is a spacer unit that connects a monomer unit and a photoreactive group, and any of those usually used in this field can be suitably used. Such spacer unit, for _{example, - (CH 2) p- (} . Here, p is an integer of 1 to 12), 1,2-propylene, 1,3-butylene, cyclopentane - 1,2-diyl, cyclopentane-1,3-diyl, cyclohexane-1,3-diyl, cyclohexane-1,4-diyl, piperidine-1,4-diyl, piperazine-1,4-diyl, 1,2 -Phenylene, 1,3-phenylene, 1,4-phenylene and the like can be mentioned. Of these spacer units, — (CH ₂ ) p — (p is an integer of 1 to 12) is preferable. As p, an integer of 3 to 9 is preferable, and an integer of 5 to 7 is more preferable, and 6 is most preferable.

Ring A is an unsubstituted or substituted alicyclic hydrocarbon or an unsubstituted or substituted aromatic ring. Of these, an unsubstituted or substituted aromatic ring is preferred, and an unsubstituted aromatic ring is more preferred. Ring B is an unsubstituted or substituted aromatic ring, and among these, an unsubstituted aromatic ring is preferred. Ring A and ring B are both divalent groups as shown in the general formula (I), but in this specification, when ring A or ring B is “unsubstituted”, these divalent groups are formed. It means “unsubstituted” in a bond other than the bond to be performed. In the present specification, when ring A and ring B are exemplified by structural formulas, the bond on the main chain side is on the left side, and the bond on the side chain end side is on the left side. It shall be written so that it is on the right side. The ring A substituent (X ^{1A to} X ^42A ) and the ring B substituent (X ^{1B to} X ^40B ) are each independently a group selected from an alkyl group, an alkoxy group, a cyano group, a nitro group, and a halogen atom. Among them, an alkoxy group is preferable. Ring A or ring B as a whole has one or more substituents, respectively. The preferred number of substituents for ring A or ring B is 1.

The Z, an alkyl group, an alkoxy group, a cyano group, a nitro group, a halogen ^{atom, -CH = CHZ 1, -C≡CZ 1} ( where, Z ¹ is an alkyl group, alkoxy group, alkoxycarbonyl group, alkoxy sulfonyl group, A cyano group, a nitro group or a halogen atom), —COOZ ² , or —SO ₃ Z ² (wherein Z ² is an alkyl group), among which an alkoxy group is preferred. Of these, Z ¹ is preferably an alkoxy group.
Examples of R include a hydrogen atom, a methyl group, a phenyl group, and a chlorine atom. Among these, a hydrogen atom and a methyl group are preferable.
n is preferably 0.

  In the present specification, examples of the alkyl group include alkyl groups having 1 to 12 carbon atoms. Among them, those having 1 to 6 carbon atoms are preferable, and those having 1 to 4 carbon atoms are more preferable. Includes a methyl group. Examples of the alkoxy group include an alkoxy group having 1 to 12 carbon atoms. Among them, an alkoxy group having 1 to 6 carbon atoms is preferable, an alkoxy group having 1 to 4 carbon atoms is more preferable, and a methoxy group is most preferable. It is done. Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom, and among these, a fluorine atom is preferable.

〔式中，記号は前記と同一意味を有する。〕
で示されるモノマーを，無溶媒又は溶媒中で，重合させることにより製造することができる。Ｍが１種のモノマー単位を表す場合，これを重合して得られる一般式（Ｉ）の光反応性ポリマーはホモポリマーとなり，一方，Ｍが２種以上のモノマー単位を表す場合，一般式（Ｉ）の光反応性ポリマーは，それら複数種のモノマー単位が重合したコポリマーとなる。重合は，光又は熱を用いて実施することができる。重合工程において，該モノマーや溶媒等を仕込む方法は特に限定されず，重合前に反応容器へ予め全材料を投入した後に重合を開始してもよいし，該モノマーや溶媒等の一部について重合開始した後に，残りを滴下又は分割投入などの方法により段階的に追加してもよい。 The photoreactive polymer (I) according to the present invention has the general formula (II)

[Wherein the symbols have the same meaning as described above. ]
Can be produced by polymerizing the monomer represented by the formula without a solvent or in a solvent. When M represents one type of monomer unit, the photoreactive polymer of the general formula (I) obtained by polymerizing the monomer unit is a homopolymer, whereas when M represents two or more types of monomer units, the general formula ( The photoreactive polymer of I) is a copolymer obtained by polymerizing these plural types of monomer units. The polymerization can be carried out using light or heat. In the polymerization step, the method of charging the monomer, solvent, etc. is not particularly limited, and the polymerization may be started after all materials are charged into the reaction vessel before polymerization, or a part of the monomer, solvent, etc. is polymerized. After starting, the remainder may be added stepwise by a method such as dripping or split charging.

  In addition, although not essential for the polymerization of the monomer (II), other monomers may be contained, and such a monomer is a compound having a polymerizable unsaturated bond (for example, an ethylenically unsaturated bond). As long as it is, it is not particularly limited in other respects, and it may be a compound having liquid crystallinity or a compound having no liquid crystallinity.

  Examples of such monomers include methyl (meth) acrylate, t-butyl (meth) acrylate, stearyl (meth) acrylate, cyclohexyl (meth) acrylate, ethoxyethyl (meth) acrylate, hydroxyethyl (meth) acrylate, and phenyl. (Meth) acrylate, (meth) acrylic monomers such as N, N-dimethylacrylamide, styrene, α-methylstyrene, p-styrenesulfonic acid, ethyl vinyl ether, N-vinyl imidazole, vinyl acetate, vinyl pyridine, 2-vinyl naphthalene , Vinyl chloride, vinyl fluoride, N-vinylcarbazole, vinylamine, vinylphenol, vinyl monomers such as N-vinyl-2-pyrrolidone, 4-allyl-1,2-dimethoxybenzene, 4-ary Phenol, 4-allyl-based monomers such as methoxy allyl benzene, phenyl maleimide, maleimide such as cyclohexyl maleimide. Any of these monomers may be used alone, or two or more of these monomers may be used in combination.

  When polymerizing in solution, a general-purpose organic solvent can be used without any particular limitation. Specific examples of the solvent include alcohol solvents such as ethanol, propanol and butanol, ketone solvents such as acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone and cyclopentanone, ethyl acetate, butyl acetate, propylene glycol monomethyl ether acetate and the like. Ester solvents, ether solvents such as diethyl ether and diglyme, hydrocarbon solvents such as hexane, cyclohexane, methylcyclohexane, toluene and xylene, nitrile solvents such as acetonitrile, amide solvents such as N-methylpyrrolidone and dimethylacetamide Etc. Any of these solvents may be used alone or in combination of two or more.

  In the above polymerization, a photopolymerization initiator can be used. As the photopolymerization initiator, any general-purpose photopolymerization agent generally known for forming a uniform film by irradiation with a small amount of light can be used. Specific examples include, for example, azonitrile photopolymerization initiators such as 2,2′-azobisisobutyronitrile (AIBN) and 2,2′-azobis (2,4-dimethylvaleronitrile), Irgacure 907 (Ciba Α-Aminoketone photopolymerization initiators such as Specialty Chemicals Co., Ltd., Irgacure 369 (Ciba Specialty Chemicals Co., Ltd.), 4-phenoxydichloroacetophenone, 4-t-butyl-dichloroacetophenone, diethoxyacetophenone, 1 -(4-Isopropylphenyl) -2-hydroxy-2-methylpropan-1-one, 1-hydroxycyclohexyl phenyl ketone, 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butane-1 -Acetophenone photopolymerization initiators such as ON, benzoin, Benzoin photopolymerization initiators such as benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, and benzyldimethyl ketal, benzophenone, benzoylbenzoic acid, methyl benzoylbenzoate, 4-phenylbenzophenone, hydroxybenzophenone, acrylated benzophenone, 4-benzoyl Benzophenone photopolymerization initiators such as -4'-methyldiphenyl sulfide, thioxanthone photopolymerization initiators such as 2-chlorothioxanthone, 2-methylthioxanthone, isopropylthioxanthone, 2,4-diisopropylthioxanthone , 2,4,6-trichloro-s-triazine, 2-phenyl-4,6-bis (trichloromethyl) -s-triazine, 2- (p-methoxyphenyl) -4,6-bis (trick (Loromethyl) -s-triazine, 2- (p-tolyl) -4,6-bis (trichloromethyl) -s-triazine, 2-piperonyl-4,6-bis (trichloromethyl) -s-triazine, 2,4 -Bis (trichloromethyl) -6-styryl-s-triazine, 2- (naphth-1-yl) -4,6-bis (trichloromethyl) -s-triazine, 2- (4-methoxy-naphth-1-) Yl) -4,6-bis (trichloromethyl) -s-triazine, 2,4-trichloromethyl- (piperonyl) -6-triazine, 2,4-trichloromethyl (4′-methoxystyryl) -6-triazine, etc. Triazine photopolymerization initiators, carbazole photopolymerization initiators, imidazole photopolymerization initiators, etc .; and α-acyloxy esters, acylphosphine oxides Methylphenylglyoxylate, benzyl, 9,10-phenanthrenequinone, camphorquinone, ethylanthraquinone, 4,4'-diethylisophthalophenone, 3,3 ', 4,4'-tetra (t-butylper And photopolymerization initiators such as oxycarbonyl) benzophenone, 4,4′-diethylaminobenzophenone, and thioxanthone. Any of the photopolymerization initiators may be used alone, or two or more of them may be used in combination.

  The temperature during the polymerization varies depending on the type of monomer (II), the type of polymerization solvent, the type of initiator, and the like, but is preferably in the range of 40 to 150 ° C, more preferably 50 to 120 ° C.

  The photoreactive polymer (I) according to the present invention thus obtained is usually contained in a polymerizable composition that causes polymerization by light and heat, in addition to a photopolymerization initiator, a surfactant, a solvent, and the like. Components can be appropriately added to obtain a composition for a photo-alignment film. The content of these optional components is not particularly limited, but usually about 1 to about 10% by weight of the photopolymerization initiator and about 0.1 to about 5% by weight of the surfactant based on the total weight of the polymer (I). The solvent is preferably contained in an amount of about 70 to about 99% by weight.

As the photopolymerization initiator, those described above can be used in the same manner.
As the surfactant, any surfactant generally used for forming a uniform film can be used. Specific examples include, for example, sodium lauryl sulfate, ammonium lauryl sulfate, triethanolamine lauryl sulfate, polyoxyethylene alkyl ether sulfate, alkyl ether phosphate, sodium oleyl succinate, potassium myristic acid, potassium coconut oil fatty acid, sodium lauroyl monkey Anionic surfactants such as cosinates; Nonionic surfactants such as polyethylene glycol monolaurate, sorbitan stearate, glyceryl myristate, glyceryl dioleate, sorbitan stearate, sorbitan oleate; stearyltrimethylammonium chloride, behenyl chloride Chaotic properties such as trimethylammonium, stearyldimethylbenzylammonium chloride, cetyltrimethylammonium chloride, etc. Activators; amphoteric surfactants such as alkylbetaines such as lauryl betaine, alkylsulfobetaine, cocamidopropyl betaine, alkyldimethylaminoacetic acid betaine, alkylimidazolines, sodium lauroyl sarcosine, sodium cocoamphoacetate; and BYK-361, BYK -306, BYK-307 (manufactured by Big Chemie Japan Co., Ltd.), Florard FC430 (manufactured by Sumitomo 3M Co., Ltd.), Megafac F171, R08 (manufactured by Dainippon Ink & Chemicals, Inc.) and the like. Any of these surfactants may be used alone, or two or more thereof may be used in combination.

  As the solvent, any solvent usually used in this field can be used, and specific examples of such solvents include toluene, ethylbenzene, ethylene glycol monomethyl ether, ethylene glycol dimethyl ether, propylene glycol methyl ether, dibutyl ether. , Acetone, methyl ethyl ketone, ethanol, propanol, cyclohexane, cyclopentanone, methylcyclohexane, tetrahydrofuran, dioxane, cyclohexanone, n-hexane, ethyl acetate, butyl acetate, propylene glycol methyl ether acetate, methoxybutyl acetate, N-methylpyrrolidone, dimethyl Examples include acetamide. Any of these may be used alone or in combination of two or more.

  The composition for a photo-alignment film of the present invention thus obtained is applied to a substrate, and after removing the solvent as necessary, it can be made into a photo-alignment film by irradiating it with linearly polarized light. .

  As a base material constituting the substrate, for example, glass base materials such as quartz glass, alkali glass, non-alkali glass, polyimide, polyamide, acrylic resin, polyvinyl alcohol, triacetyl cellulose, polyethylene terephthalate, cycloolefin polymer, polyethylene, polycarbonate Resin base materials such as polystyrene and poly (trifluorotrifluoroethylene), and metal base materials such as iron, aluminum and copper, and glass base materials are more preferable.

  As a coating method of the composition for photo-alignment films, any method generally known in the art may be used. For example, spin coating method, bar coating method, die coater method, screen printing method, spray coater method, etc. There is.

  The drying step may be performed by any method commonly used in this field, and is not particularly limited as long as the resin layer film is formed.

  Linearly polarized light can be irradiated from either a vertical direction or an oblique direction with respect to the film, but is preferably irradiated from a vertical direction.

  In the present invention, linearly polarized light is light in which a plane including the vibration direction of an electric field (or magnetic field) is specified as one. Linearly polarized light can be obtained by using a polarizing filter or polarizing prism for the light from the light source. The irradiation light can be an infrared ray, visible ray, ultraviolet ray (near ultraviolet ray, far ultraviolet ray, etc.), X-ray, charged particle beam (for example, electronic electricity), etc., as long as it can cause a chemical reaction by irradiation. Although not particularly limited, usually, the irradiation radiation often has a wavelength of 200 nm to 500 nm, and from the viewpoint of efficiency, near ultraviolet light of 350 nm to 450 nm is preferable. Examples of the light source include a xenon lamp, a high pressure mercury lamp, an ultra high pressure mercury lamp, and a metal halide lamp. Ultraviolet light or visible light obtained from such a light source may be irradiated with an interference filter, a color filter, or the like to limit the wavelength range of irradiation.

Radiation energy may vary depending on the type and thickness of the photoreactive polymer (I), usually from about ^{10mJ / cm 2 ~5000mJ / cm 2} . For example, a thin film having a thickness of about 100 nm comprising poly [1- [6- [4- [4- [4- (methoxy) phenoxycarbonyl] phenoxy] hexyloxycarbonyl] -1-methylethylene] synthesized in Example 1 was used. In this case, it is about 250 to 4000 mJ / cm ² .

  In addition, if a photomask is used when irradiating linearly polarized light, alignment ability of liquid crystal or the like can be generated in the photo-alignment film in a pattern in two or more different directions. Specifically, after applying and drying the composition for a photo-alignment film of the present invention, a photomask is placed on the composition and irradiated with linearly polarized light to give alignment ability only to the exposed portion, and if necessary, direction By repeating this a plurality of times, orientation ability can be generated in a pattern in a plurality of directions.

  The film thickness of the photo-alignment film of the present invention is preferably about 10 to about 500 nm, more preferably about 100 to about 500 nm, and still more preferably about 100 to about 200 nm.

  A liquid crystal compound (including a liquid crystal compound that is a dye and a liquid crystal compound that is a conductive compound) is prepared on the photo-alignment film thus obtained. After aligning the liquid crystalline compound by heating to a temperature at which the liquid crystalline state is exhibited, the liquid crystalline compound is further cooled to a temperature below the temperature at which the liquid crystalline compound exhibits the liquid crystalline state, thereby fixing the alignment state of the liquid crystalline compound. Various optical materials such as retardation films, viewing angle enhancement films, brightness enhancement films, polarizing films, and other optical anisotropic films, conductive materials, nonlinear optical materials, photoreactive actuators, etc. can do. When applying a liquid crystalline compound, it may be dissolved in a solvent and applied as desired. As such a solvent, any solvent usually used in this field can be used. Specifically, those described above, that is, toluene, ethylbenzene, ethylene glycol monomethyl ether, ethylene glycol dimethyl ether, propylene glycol methyl ether, dibutyl ether, acetone, methyl ethyl ketone, ethanol, propanol, cyclohexane, cyclopentanone, methylcyclohexane, tetrahydrofuran , Dioxane, cyclohexanone, n-hexane, ethyl acetate, butyl acetate, propylene glycol methyl ether acetate, methoxybutyl acetate, N-methylpyrrolidone, dimethylacetamide and the like. Any of these may be used alone or in combination of two or more.

  In the case of dyes or conductive compounds that are not liquid crystalline compounds, these dyes or conductive compounds are mixed with liquid crystal compounds and treated in the same manner as described above, or these dyes or conductive compounds are dissolved in a solvent. Various optical anisotropic films and optical materials can also be produced by applying this onto the photo-alignment film and drying it.

  Here, as the liquid crystal compound, the dye, and the conductive compound, any of those usually used in this field can be suitably used. For example, the liquid crystalline compound includes cyanobiphenyl type nematic liquid crystal. Examples of the dye include azo dyes (polyazo dyes, disazo dyes, etc.), dichroic dyes such as anthraquinone dyes, and the like. Examples of the conductive compound include oligothiophene and polythiophene. Moreover, as a solvent, the above-mentioned thing quoted as a solvent at the time of apply | coating a liquid crystalline compound can be used similarly.

  The thickness of the optically anisotropic film and optical material of the present invention obtained in this way varies depending on the application, etc., but in general, the range of 0.1 to 20.0 μm is preferable, and 1.0 to The range of 5.0 μm is more preferable.

  Further, if the photo-alignment film of the present invention is used, a liquid crystal cell including the photo-alignment film can be produced. For example, the two light alignment films have a predetermined angle between the direction of the polarization axis when linearly polarized light is irradiated on one light distribution film and the direction of the polarization axis when linearly polarized light is irradiated on the other light distribution film. (E.g., 90 [deg.] Or any angle between 180 [deg.] And 270 [deg.]), And a liquid crystal cell is manufactured by filling a liquid crystal compound between the opposed photo-alignment films. Can do.

  The photoreactive polymer (I) according to the present invention is prepared by appropriately adding components usually contained in a polymerizable composition that causes polymerization by light and heat in addition to a photopolymerization initiator, a surfactant, a solvent, and the like. It can be set as the composition for anisotropic films. The content of these optional components is not particularly limited, but is usually about 1 to about 5% by weight of the photopolymerization initiator and about 0.1 to about 1% by weight of the surfactant based on the total weight of the polymer (I). The solvent is preferably contained in an amount of about 50 to about 80% by weight. As optional components such as a photopolymerization initiator, a surfactant, and a solvent, those described for the composition for photo-alignment films can be used in the same manner. However, the photoreactive polymer (I) is usually a liquid crystal compound, but when the other monomer added during the polymerization of the monomer (II) is a compound that does not exhibit liquid crystallinity, Depending on the amount of the monomer added, the polymer (I) can be a compound that does not exhibit liquid crystallinity. When the polymer (I) is a compound that does not exhibit liquid crystallinity, a part of the polymer (I) is replaced with a liquid crystal compound in the preparation of the composition for optically anisotropic film, and the optical Liquid crystallinity is shown as the whole composition for anisotropic films. As the liquid crystal compound added in this manner, any of those usually used in this field can be used. For example, a liquid crystal compound composed of rod-like molecules is preferable, or a nematic liquid crystal is preferable.

  A composition obtained by coating the substrate for the optically anisotropic film composition of the present invention thus obtained is irradiated with linearly polarized light, and then the liquid crystalline compound contained in the optically anisotropic film composition is a liquid crystal. The liquid crystalline compound is aligned by heating to a temperature at or above the temperature indicating the state, and further, the alignment state is fixed by cooling to a temperature below the temperature at which the liquid crystalline compound exhibits the liquid crystal state. Can be produced.

  The base material constituting the substrate, the coating method, irradiation with linearly polarized light, and the like are all the same as the production of the photo-alignment film. The thickness range of the obtained optically anisotropic film is the same as that exemplified for the optically anisotropic film.

  EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated concretely, this invention is not limited to the following Example from the first.

1. Synthesis of 4- (6-hydroxyhexyloxy) benzoic acid

100.0 g (0.7 mol) of 4-hydroxybenzoic acid and 105.1 g (1.6 mol) of potassium hydroxide were dissolved in 400.0 g of water. To this solution, 108.8 g (0.8 mol) of 6-chlorohexanol was added dropwise over 1 hour. Subsequently, it heated and refluxed at 100 degreeC. After 20 hours, the reaction mixture was cooled and 344.6 g (1.7 mol) of 35% hydrochloric acid was added dropwise at room temperature with vigorous stirring. The precipitated solid was collected by filtration and recrystallized from 400 g of tetrahydrofuran (THF) to obtain 120.0 g (0.5 mol) of the title compound as white crystals.
Yield 69.5%, melting point 135-140 ° C.

2. Synthesis of 4- [6- (2-methylacryloyloxy) hexyloxy] benzoic acid

120.0 g (0.5 mol) of the compound obtained in 1 above and 81.5 g (0.8 mol) of triethylamine were dissolved in 480.0 g of THF. To this solution, 84.2 g (0.8 mol) of methacrylic acid chloride was added dropwise over 1 hour. It was then heated to 40 ° C. After 4 hours, the reaction solution was cooled and 240.0 g of water was added. To the separated organic layer, 367.2 g (1 mol) of 10% hydrochloric acid was added and stirred. The separated organic layer was concentrated, and the residue was recrystallized with 400.0 g of toluene to obtain 96.0 g (0.3 mol) of the title compound as white crystals.
Yield 62.2%, melting point 81 ° C.

3. Synthesis of 4- [6- (2-methylacryloyloxy) hexyloxy] thiobenzoic acid S-4- (methoxy) phenyl ester

96.0 g (0.3 mol) of the compound obtained in 2 above, 42.1 g (0.3 mol) of 4-methoxythiophenol and 7.7 g (0.1 mol) of N, N-dimethylaminopyridine were added to 960 g of dichloromethane. Dissolved in. To this solution, 71.1 g (0.3 mol) of dicyclohexylcarbodiimide (DCC) was added. After reacting for 2 hours at room temperature, 288 g of water was added. The separated organic layer was concentrated, and the residue was recrystallized from 100 g of toluene to obtain 110 g (0.3 mol) of the title compound as white crystals.
Yield 85.6%, melting point 56 ° C.

4). Synthesis of poly [1- [6- [4- [4- (methoxy) phenylthiocarbonyl] phenoxy] hexyloxycarbonyl] -1-methylethylene]

  110 g (0.2 mol) of the compound obtained in 3 above and 0.8 g (5 mmol) of AIBN were dissolved in 412 g of cyclohexanone. Nitrogen was bubbled through the solution for 1 hour. It was then heated to 80 ° C. After 10 hours, the reaction solution was cooled and added dropwise to 346 g of normal hexane at room temperature with vigorous stirring. The separated polymer was collected by filtration and dried at 50 ° C. under reduced pressure to obtain 93.5 g of the title polymer. Yield 85%.

(Measurement of weight average molecular weight (MW))
The weight average molecular weight (MW) of the polymer obtained above was measured using gel filtration chromatography (GPC). The weight average molecular weight (MW) obtained was 21000.

(Measurement of phase transition temperature)
It was 45-125 degreeC when the phase transition temperature of the polymer obtained above was measured using the differential scanning calorimetry (DSC).

5). Preparation of Composition for Photoalignment Film 5 g of the polymer obtained above was dissolved in 95 g of THF to obtain Composition 1 for photoalignment film.

6). Production of photo-alignment film The composition 1 for photo-alignment film obtained above was applied on a quartz glass substrate so as to be a thin film having a thickness of about 100 nm using a spin coater and dried. The obtained substrate was irradiated with ultraviolet rays (10 mW / cm ² ) converted into linearly polarized light using a Grand Taylor prism for 200 seconds from the direction perpendicular to the substrate, and a photo-alignment film was produced on the substrate.

(Confirmation of photocleavage of thiobenzoate skeleton)
In order to confirm that photo-cleavage of the thiobenzoate (ester) skeleton and eventually photo-fleece rearrangement occurred by linearly polarized light irradiation, the change of the thin film when irradiated with linearly polarized light was observed in the same way as above. Observed by spectroscopy. The results are as shown in the chart of FIG.
As is clear from the figure, the absorption peak due to sulfur atoms in the vicinity of 1670 cm ⁻¹ decreased with the irradiation of linearly polarized light, and the thiobenzoate skeleton partially disappeared due to photocleavage. Can be read.
On the other hand, the absorption peak due to the carbonyl group of the ketone near 1700 to 1730 cm ⁻¹ is increased by the irradiation with linearly polarized light, and the absorption peak due to the carbonyl group of the ketone increases according to the irradiation dose. It can be seen that it has undergone photocleavage and photofleece rearrangement to convert to the carbonyl group of the ketone.

(Evaluation of photo-alignment)
A liquid crystal cell was prepared by facing the two substrates with the photo-alignment film obtained above so that their polarization axes would be parallel when irradiated with linearly polarized ultraviolet rays. Liquid crystal E7 (manufactured by Merck Japan) in which the dye Disperse Blue 14 (manufactured by Aldrich) was dispersed was filled, heated to 80 ° C. to make the liquid crystal isotropic phase, and then cooled to room temperature.
When this liquid crystal cell was observed with a polarizing microscope, it was confirmed that the liquid crystal was aligned in a direction perpendicular to the polarization axis of the irradiated linearly polarized light.

7). Manufacture of liquid crystal cell A liquid crystal cell was prepared by facing the two substrates with the photo-alignment film obtained in 6 above so that the polarization axes when orthogonally polarized ultraviolet rays were irradiated were perpendicular to each other. The liquid crystal E7 was filled to prepare a TN type liquid crystal cell.
It was confirmed that the liquid crystal cell was correctly driven by applying a voltage between both substrates of the TN type liquid crystal cell.

8). Preparation of Composition for Optical Anisotropic Film 5 g of the polymer obtained in 4 above was dissolved in 15 g of THF to obtain Composition 1 for optical anisotropic film.

9. Production of Optically Anisotropic Film Composition 1 for optically anisotropic film was applied on a glass substrate to a thickness of about 1.2 μm using a spin coater and dried. The obtained substrate was irradiated with ultraviolet rays (10 mW / cm ² ) converted into linearly polarized light using a Grand Taylor prism from the vertical direction for 200 seconds. The substrate was heated at 80 ° C. for 20 minutes and then cooled to room temperature.
When the film formed on the substrate was observed with a polarizing microscope, light and darkness was observed, confirming that an optically anisotropic film could be produced. When the birefringence of the produced optically anisotropic film was measured using an ellipsometer OPTIPRO (manufactured by Shintec Co., Ltd.), it showed a value of Δn = 0.11 and Re = 132 nm, which can be used as a retardation film. It was confirmed that there was.

10. Evaluation of colorability by exposure The composition 1 for optically anisotropic film was applied on a glass substrate so as to have a thickness of about 200 nm using a spin coater, and dried. The obtained substrate was irradiated with ultraviolet rays (10 mW / cm ² ) converted into linearly polarized light using a Grand Taylor prism from the direction perpendicular to the substrate for 300 seconds and 1200 seconds. The substrate was heated at 80 ° C. for 20 minutes and then cooled to room temperature.
The film on the glass substrate before irradiating the linearly polarized light is a “dry film” for comparison, and the film on the glass substrate irradiated with the linearly polarized light is “irradiated film 1 (300S)” according to the irradiation amount. And as "irradiated film 2 (1200S)", the transmittance | permeability was measured about each film using the light of a wavelength of 400 nm. The results are as shown in Table 1.

  From the above results, the film according to the present invention is a film in which coloring due to exposure is suppressed because the transmittance is almost the same as that before irradiation even after irradiation with linearly polarized light. I understand.

  The polymer composition for a photo-alignment film and optically anisotropic film of the present invention comprises a photoalignment film and an optically anisotropic film produced using the same, and further aligning a liquid crystalline compound or the like on the photoalignment film. It is useful as a raw material for various optical anisotropic films such as retardation films, viewing angle enhancement films, brightness enhancement films, polarizing films, etc., conductive materials, nonlinear optical materials, photoreactive actuators, etc. In addition, the optically anisotropic film and optical material obtained in this way can be used as various optical elements, particularly for display devices such as OA equipment such as computers and facsimiles, mobile phones, electronic notebooks, liquid crystal televisions, and video cameras. it can.

Claims (12)

Formula (I)

[Wherein M is a monomer unit forming the main chain of the homopolymer or copolymer, SPCR is a spacer unit, ring A is an unsubstituted or substituted alicyclic hydrocarbon or an unsubstituted or substituted aromatic ring, ring B is an unsubstituted or substituted aromatic ring, Z is an alkyl group, an alkoxy group, a cyano group, a nitro group, a halogen ^{atom, -CH = CHZ 1, -C≡CZ 1} ( where, Z ¹ is an alkyl group, an alkoxy A group, an alkoxycarbonyl group, an alkoxysulfonyl group, a cyano group, a nitro group, or a halogen atom), —COOZ ² , or —SO ₃ Z ² (wherein Z ² is an alkyl group), and n is 0 . ]
The composition for photo-alignment films which contains the photoreactive polymer which has a repeating unit shown by these.   The substituent of ring A and the substituent of ring B are each independently one or more groups selected from the group consisting of an alkyl group, an alkoxy group, a cyano group, a nitro group, and a halogen atom. Composition for photo-alignment film. M is acrylate, methacrylate, 2-chloroacrylate, 2-phenylacrylate, acryloylphenylene, acrylamide, methacrylamide, 2-chloroacrylamide, 2-phenylacrylamide, vinyl ether, styrene derivative, vinyl ester, maleic acid derivative, fumaric acid derivative. , One or more monomer units selected from the group consisting of siloxane and epoxide,
SPCR is — (CH ₂ ) p — (where p is an integer of 1 to 12), 1,2-propylene, 1,3-butylene, cyclopentane-1,2-diyl, cyclo Pentane-1,3-diyl, cyclohexane-1,3-diyl, cyclohexane-1,4-diyl, piperidine-1,4-diyl, piperazine-1,4-diyl, 1,2-phenylene, 1,3- A spacer unit selected from the group consisting of phenylene and 1,4-phenylene,
Ring A is

[However, X ^{1A to} X ^42A each independently represents a hydrogen atom, an alkyl group, an alkoxy group, a halogen atom, or a cyano group. ]
Any of the groups represented by
Ring B is

[However, X ^{1B to} X ^40B are each independently a hydrogen atom, an alkyl group, an alkoxy group, a halogen atom, or a cyano group, and X is a nitrogen atom, an oxygen atom, or a sulfur atom. ]
The composition for photo-alignment films | membranes of Claim 1 which is either group shown by these. At least one of X ^1B and X ^4B , at least one of X ^5B and X ^12B , at least one of X ^13B and X ^24B , at least one of X ^25B and X ^30B , at least one of X ^31B and X ^38B , and X ^39B The composition for photo-alignment films according to claim 3, which is a hydrogen atom. Formula (Ia)

[Wherein, R represents a hydrogen atom, a methyl group, a phenyl group or a chlorine atom, and each of X ^{1A to} X ^4A and X ^{1B to} X ^4B independently represents a hydrogen atom, an alkyl group, an alkoxy group, a halogen atom or a cyano group, Z is an alkyl group, an alkoxy group, a cyano group, a nitro group, a halogen ^{atom, -CH = CHZ 1, -C≡CZ 1} ( where, Z ¹ is an alkyl group, an alkoxy group, an alkoxy A carbonyl group, an alkoxysulfonyl group, a cyano group, a nitro group, or a halogen atom.), —COOZ ² , or —SO ₃ Z ² (wherein Z ² is an alkyl group), and p is 1 to 1 Any integer of 12 and n is 0 . ]
The composition for photo-alignment films which contains the photoreactive polymer which has a repeating unit shown by these. The composition for photo-alignment films according to claim 5, wherein at least one of X ^1B and X ^4B is a hydrogen atom. The photo-alignment film formed in the base-material surface using the composition for photo-alignment films in any one of Claims 1-6. It formed using a photo-alignment film according to claim 7, optically anisotropic fill beam. An optical material formed using the photo-alignment film according to claim 7. Formed by filling a liquid crystal compound between two optical alignment film of claim 7 which are opposed, the liquid crystal cell. Formula (I)

[Wherein M is a monomer unit forming the main chain of the homopolymer or copolymer, SPCR is a spacer unit, ring A is an unsubstituted or substituted alicyclic hydrocarbon or an unsubstituted or substituted aromatic ring, ring B is an unsubstituted or substituted aromatic ring, Z is an alkyl group, an alkoxy group, a cyano group, a nitro group, a halogen ^{atom, -CH = CHZ 1, -C≡CZ 1} ( where, Z ¹ is an alkyl group, an alkoxy A group, an alkoxycarbonyl group, an alkoxysulfonyl group, a cyano group, a nitro group, or a halogen atom), —COOZ ² , or —SO ₃ Z ² (wherein Z ² is an alkyl group), and n is 0 . ]
A composition for optically anisotropic films, comprising a photoreactive polymer having a repeating unit represented by: An optically anisotropic film formed on a substrate surface using the composition for optically anisotropic film according to claim 11 .

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